SLC67A1

Gene

solute carrier family 67 member 1

HGNCHGNC:10964 EnsemblENSG00000110628 NCBI Gene5002

Locus: gene with protein productLocation: 11p15.4

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asIMPT1 · ORCTL2 · BWSCR1A · SLC22A18 · SLC22A1L · BWR1A · TSSC5 · ITM

View full nomenclature history (13)

Previous symbolsIMPT1, ORCTL2, BWSCR1A, SLC22A18, SLC22A1L

Alias symbolsBWR1A, TSSC5, ITM

Previous namessolute carrier family 22 (organic cation transporter), member 1-like, solute carrier family 22 member 18, solute carrier family 22, member 18

Alias namesorganic cation transporter like 2, imprinted multi-membrane-spanning polyspecific transporter-like gene 1

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Diabetes Mellitus, Type 2

Diabetic Retinopathy

Lung Neoplasms

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Solute carrier family 67

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-02-05.

Open TargetsGene–disease associations from the Open Targets Platform.